Omi Manufacturing Pty., Ltd. is one of 23426 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Omi Manufacturing Pty., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: OMI RETRACTABLE SAFTEY SYRINGE, VARIOUS, PERSONNA PLUS SAFETY SCALPEL SYSTEM
2
Total
2
Cleared
0
Denied
Omi Manufacturing Pty., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Deer Field, US.
Historical record: 2 cleared submissions from 2003 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Omi Manufacturing Pty., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Omi Manufacturing Pty., Ltd.
2 devices